Canonical Allele Identifier: CA10618277

Gene: FRAS1

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.78057765C>G , CM000666.2:g.78057765C>G	GRCh38
NC_000004.11:g.78978919C>G , CM000666.1:g.78978919C>G	GRCh37
NC_000004.10:g.79197943C>G	NCBI36
NG_015812.1:g.5196C>G
NG_015812.2:g.5196C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_025074.7:c.-245C>G MANE Select	NP_079350.5:n.-245C>G
ENST00000512123.4:c.-245C>G MANE Select	ENSP00000422834.2:n.-245C>G
NM_001166133.1:c.-245C>G	NP_001159605.1:n.-245C>G
NM_001166133.2:c.-245C>G	NP_001159605.1:n.-245C>G
NM_025074.6:c.-245C>G	NP_079350.5:n.-245C>G
ENST00000325942.10:c.-245C>G	ENSP00000326330.6:n.-245C>G
ENST00000325942.11:c.-245C>G	ENSP00000326330.6:n.-245C>G
ENST00000502446.6:c.-245C>G	ENSP00000423645.2:n.-245C>G
ENST00000508900.2:c.-245C>G	ENSP00000423809.2:n.-245C>G
ENST00000508909.5:c.-245C>G	ENSP00000425583.1:n.-245C>G
ENST00000512123.3:c.-245C>G	ENSP00000422834.2:n.-245C>G
ENST00000682513.1:c.-245C>G	ENSP00000508201.1:n.-245C>G
ENST00000683711.1:n.76C>G
ENST00000684159.1:c.-245C>G	ENSP00000506875.1:n.-245C>G
XM_006714314.1:c.-245C>G	XP_006714377.1:n.-245C>G
XM_006714316.1:c.-245C>G	XP_006714379.1:n.-245C>G
XM_006714316.3:c.-245C>G	XP_006714379.1:n.-245C>G